ArticleJournal of dental research2018
Dysplasia Should Not Be Ignored in Lichenoid Mucositis.
Article in Journal of dental research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.
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Who cites it
17 citing papers in PubMed, 32 citations in OpenAlex.
- [Progress in clinicopathological diagnosis of oral potentially malignant disorders].Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology · 2025Review
- Study on the potential links between clinical features of oral lichenoid mucositis and systemic diseases.BMC oral health · 2025Article
- Cell-mediated mucositis of the oral cavity: narrative review on etiology, clinico-pathological aspects and malignant transformation.Pathologica · 2025Review
- Malignant transformation of oral lichen planus: where are we now?Medicina oral, patologia oral y cirugia bucal · 2025Review
- Controversies regarding oral lichen planus and lichenoid-dysplastic lesions.Canadian journal of dental hygiene : CJDH = Journal canadien de l'hygiene dentaire : JCHD · 2024Review
- Review
- Clinicohistological Characteristics of Patients with Oral Lichenoid Mucositis: A Retrospective Study for Dental Hospital Records.Journal of clinical medicine · 2023Article
- Review
- Exploring the microbiome of oral epithelial dysplasia as a predictor of malignant progression.BMC oral health · 2023Article
- Predicting Progression of Low-Grade Oral Dysplasia Using Brushing-Based DNA Ploidy and Chromatin Organization Analysis.Cancer prevention research (Philadelphia, Pa.) · 2021Article
- Dysplasia in oral lichen planus: relevance, controversies and challenges. A position paper.Medicina oral, patologia oral y cirugia bucal · 2021Review
- Basement membrane degeneration is common in lichenoid mucositis with dysplasia.Canadian journal of dental hygiene : CJDH = Journal canadien de l'hygiene dentaire : JCHD · 2021Article
- Intraepithelial Macrophage Expressing CD163 Is a Histopathological Clue to Evaluate the Malignant Potency of Oral Lichenoid Condition: A Case Report and Immunohistochemical Investigation.Diagnostics (Basel, Switzerland) · 2020Article
- Clinicopathological and prognostic characterization of oral lichenoid disease and its main subtypes: A series of 384 cases.Medicina oral, patologia oral y cirugia bucal · 2020Article
- The natural history of oral mucosal lesions with both lichenoid and epithelial dysplastic features: a systematic review.Translational cancer research · 2020Article
- Incidence of squamous cell carcinoma in oral lichen planus: a 25-year population-based study.International journal of dermatology · 2019Article
- Study on thyroid autoimmunity of oral lichen planus and oral lichenoid mucositis.Journal of oral and maxillofacial pathology : JOMFPArticle
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7 authors at 3 institutions in 1 country.
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Abstract
Oral lichen planus is categorized as a potentially malignant condition by the World Health Organization; however, some argue that only lichen planus with dysplasia have malignant potential. Many pathologists call lichen planus with dysplasia "dysplasia with lichenoid mucositis (LM)" or "LM with dysplasia." Previous research has shown that certain high-risk patterns of loss of heterozygosity (LOH) in dysplastic lesions are associated with significantly increased cancer risk. However, LM without dysplasia lacks such molecular patterns, supporting the hypothesis that LM, by itself, is not potentially malignant and that only those with dysplasia have malignant potential. To further investigate the premalignant nature of LM with dysplasia, this study compared the rate of malignant progression of dysplasia with LM with that of dysplasia without LM. Patients from a population-based prospective cohort study with >10 y of follow-up were analyzed. Study eligibility included a histological diagnosis of a primary low-grade dysplasia with or without LM. A total of 446 lesions in 446 patients met the selection criteria; 373 (84%) were classified as dysplasia without LM, while 73 (16%) were classified as dysplasia with LM. Demographic and habit information, clinical information, and outcome (progression) were compared between the 2 groups. Forty-nine of 373 cases of dysplasia (13%) progressed compared to 8% (6/73) of dysplasia with LM. However, the difference was not statistically different ( P = 0.24). The 3- and 5-y rate of progression did not differ between the groups (6.7% and 12.5% for dysplasia without LM and 2.9% and 6.6% for those with LM; P = 0.36). Progression was associated with nonsmoking, location at a high-risk site, and diagnosis of moderate dysplasia regardless of whether LM was present or not. Dysplasia with or without LM had similar cancer risk, and dysplasia should not be discounted in the presence of LM.
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